Method for preparing graphene

ABSTRACT

A method of preparing graphene includes supplying a gas on a metal catalyst, the gas including CO 2 , CH 4 , and H 2 O, and reacting and cooling the resultant.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a divisional application of U.S. application Ser.No. 14/202,728, filed on Mar. 10, 2014, which claims priority to and thebenefit of Korean Patent Application No. 10-2013-0025846 filed in theKorean Intellectual Property Office on Mar. 11, 2013, the entirecontents of each of which are incorporated herein by reference.

BACKGROUND

1. Field

Example embodiments provide a method of preparing graphene and agraphene particle manufactured in accordance with this method.

2. Description of the Related Art

Graphene is a conductive material having a two-dimensional honeycombarrangement of carbon atoms and a thickness of one atom layer.

The graphene forms graphite when three-dimensionally piled, carbonnanotubes when one-dimensionally rolled, and fullerene whenzero-dimensionally shaped into a ball, and thus has been regarded as animportant model for researching various low-dimensional nano-phenomena.

The graphene is predicted to not only be structurally and chemicallyvery stable but also so conductive that it can transfer electrons 100times as fast as silicon and flow a current about 100 times as fast ascopper.

These predicted characteristics of the graphene have been experimentallyproved, since a method of separating graphene from graphite wasdiscovered in 2004, which thrilled scientists all over the world forseveral years.

The graphene is formed of a relatively light element, carbon, and iseasily processed into a one- or two-dimensional nanopattern, which maynot only be used to adjust semiconductor-conductor properties, but alsobe vastly applied to functional devices (e.g., sensors and/or memories)by using various chemical bonds of the carbon.

Accordingly, a technology using the graphene draws a lot of attention,but a method of massively producing the graphene with a relatively lowcost, a large area, and reproducibility has not yet been developed.

In general, the graphene may be prepared in five methods. A first methodis mechanical or chemical peeling or breaking large graphite into piecesand thus forming a monolayer, but it is difficult to prepare graphenehaving a large area.

A second method is epitaxy synthesis of raising carbon adsorbed orincluded in a crystal at a relatively high temperature into graphene onthe surface thereof to form graphene having a large area, but has adrawback of needing an expensive substrate device and bringing aboutrelatively insufficient electrical characteristics.

In addition, an organic synthesis method may use tetraphenyl benzene,but has drawbacks of being difficult to produce graphene having a largearea and it is expensive.

Lastly, a chemical vapor deposition method synthesizes graphene bydepositing a transition metal (Ni or Cu) catalyst layer on a substratethat adsorbs carbon well, reacting the substrate having the catalystlayer with a mixed gas of CH₄ and hydrogen at a relatively hightemperature (1000° C.) so that carbon in an appropriate amount is meltedor adsorbed in the catalyst layer, and then cooling the carbon melted oradsorbed in the catalyst layer on the substrate by using a meltingtemperature difference between the catalyst and the carbon.

However, this method has a drawback of separating the catalyst layer andthe graphene layer with a relatively high cost at a relatively highreaction temperature.

In addition, the method has difficulties in regulating reaction time ofmethane and hydrogen gas, a cooling rate, concentration of a reactiongas, and/or thickness of a catalyst layer, and continuously performing aprocess.

SUMMARY

Example embodiments provide a method of preparing graphene withrelatively high efficiency at a relatively low reaction temperature.

Example embodiments provide a nanoparticle including the grapheneprepared according to the method of example embodiments.

Example embodiments provide a patterned graphene or graphene sheetprepared according to the method of example embodiments.

According to example embodiments, a method of preparing grapheneincludes supplying a gas to a metal catalyst, the gas including CO₂,CH₄, and H₂O, reacting while heating, and cooling the resultant.

The metal catalyst may include at least one metal selected from Ni, Co,Cu, Fe, Rh, Ru, Pt, Au, Al, Cr, Mg, Mn, Mo, Si, Sn Ta, Ti, W, U, V, Zr,brass, bronze, stainless steel, and Ge, or an alloy including two ormore of the aforementioned metals.

The CH₄:CO₂:H₂O gases may be mixed in a mole ratio of about1:0.20-0.50:0.01-1.45. The CH₄:CO₂:H₂O gases may be mixed in a moleratio of about 1:0.25-0.45:0.10-1.35. The CH₄:CO₂:H₂O gases may be mixedin a mole ratio of about 1:0.30-0.40:0.50-1.0.

The reacting may heat the resultant at about 400 to about 900° C. Thecooling may cool the resultant at a given rate in the presence of aninert gas. The metal catalyst may be supported by a porous carrier ofone of Al₂O₃, SiO₂, zeolite, TiO₂, and silicon.

The metal catalyst may be supported by the porous carrier while beingbonded thereto to form a metal catalyst-porous carrier composite. Themetal catalyst may be in a form of a nanoparticle.

Alternatively, the metal catalyst may be in a form of one of a film anda substrate, and a carrier supporting the metal catalyst may be on atleast one part of the metal catalyst in the form of one of the film andthe substrate. The metal catalyst may be in the form of one of a Ni filmand the substrate. The carrier on at least one part of the metalcatalyst may be in an ionic form of one of Al, Si and Ti. The carrier onat least one part of the metal catalyst may be provided in a patternedform.

According to example embodiments, a method of manufacturing asemiconductor circuit may include the method of example embodiments,wherein the carrier may be provided in a patterned form on at least onepart of the metal catalyst in a form of one of the film and thesubstrate.

According to example embodiments, a graphene-encapsulated metalnanoparticle may be prepared in accordance with the method of exampleembodiments.

The metal nanoparticle may include at least one metal selected from Ni,Co, Cu, Fe, Rh, Ru, Pt, Au, Al, Cr, Mg, Mn, Mo, Si, Sn, Ta, Ti, W, U, V,Zr, brass, bronze, stainless steel, and Ge, or an alloy including two ormore the foregoing metals. The metal nanoparticle may have a diameter ofabout 1 to about 50 nm. The graphene-encapsulated metal nanoparticle maybe used in one of a light emitting material for a display, an electrodematerial of a battery or a solar cell, and an in vivo drug deliverymaterial.

According to example embodiments, a hollow graphene nanoparticleprepared by removing the metal nanoparticle from thegraphene-encapsulated metal nanoparticle may be prepared according tothe method of example embodiments.

The graphene may be made up of one sheet to five sheets.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic view showing a supported form of a catalyst forgraphene growth on a carrier, and the left of which is a cross-sectionalview showing catalyst metal particles physically adsorbed on thecarrier, while the right thereof is a cross-sectional view showing thecarrier and a catalyst metal bonded in a form of an alloy.

FIG. 2(a) is an exaggerated enlarged view of a catalyst metal particlein a catalyst supported by physically adsorbing a catalyst metal on aporous carrier.

FIG. 2(b) is an exaggerated enlarged view of a catalyst metal particlein another catalyst supported by alloying a catalyst metal and acarrier.

FIG. 3 is a schematic view showing different states in which carbonatoms absorbed in a catalyst layer move toward the surface of thecatalyst layer depending on the cooling rate, when graphene is preparedin a conventional chemical vapor deposition method.

FIG. 4 is a schematic view showing a process in which carbon atomsources (CO₂ and CH₄) interact with water on the surface of a catalyst,and extra carbon atoms from the carbon atom sources and the water areconverted into CO and H₂ gases and evaporated.

FIG. 5(a) is a schematic view showing a state in which the extra carbonatoms are not accumulated on the surface of a catalyst but are absorbedinto a catalyst layer and thus form a catalyst interstitial layer.

FIG. 5(b) is a schematic view showing a state in which the catalystinterstitial layer escapes onto the surface of the catalyst layer bycooling to form graphene.

FIG. 6 is a schematic view showing a process in which graphene is formedaccording to the Al ion pattern on a Ni film according to exampleembodiments.

The Ni film may be removed from the patterned graphene on the Ni film,obtaining the patterned graphene.

FIG. 7 is a 3D TEM image showing a metal catalyst for graphene growthsupported on a porous carrier according to Preparation Example 1.

FIG. 8 is a 3D TEM image showing a metal catalyst for graphene growthsupported on a porous carrier according to Preparation Example 2.

FIG. 9 is a TEM photograph showing the metal catalyst for graphenegrowth according to Preparation Example 1 after a reaction of forminggraphene on the catalyst.

FIG. 10 is a TEM photograph showing the catalyst for graphene growthaccording to Preparation Example 2 after a reaction forming graphene onthe catalyst.

FIG. 11 is a Raman graph showing that graphene is formed after thereactions of forming graphene on a catalyst for graphene growthaccording to Preparation Examples 1 and 2.

FIG. 12 is an XPS graph showing that graphene is formed after thereactions of forming graphene on a catalyst for graphene growthaccording to Preparation Examples 1 and 2.

FIG. 13 is a SEM photograph showing that graphene is formed on an Alion-coated catalyst on a Ni film according to Preparation Example 3.

FIG. 14 is a Raman graph showing that graphene is formed on a part whereAl ions are coated out of the Al ion-coated catalyst on a Ni filmaccording to Preparation Example 3.

FIG. 15 is an XPS graph showing that graphene is formed on a part whereAl ions are coated out of the Al ion-coated catalyst on a Ni filmaccording to Preparation Example 3.

FIG. 16 is a Raman graph showing that graphene is formed on a Nicatalyst deposited on a semiconductor wafer according to PreparationExample 4.

FIG. 17(a) is a SEM photograph showing that the graphene is formed on aNi catalyst deposited on a semiconductor wafer according to PreparationExample 4.

FIG. 17(b) is an enlargement of FIG. 17(a).

DETAILED DESCRIPTION

The inventive concepts will now be described more fully with referenceto the accompanying drawings, in which example embodiments are shown. Inthe drawings, the same reference numerals denote the same elements, andsizes or thicknesses of elements may be exaggerated for clarity.

It will be understood that when an element is referred to as being“connected” or “coupled” to another element, it can be directlyconnected or coupled to the other element or intervening elements may bepresent. In contrast, when an element is referred to as being “directlyconnected” or “directly coupled” to another element, there are nointervening elements present. As used herein the term “and/or” includesany and all combinations of one or more of the associated listed items.

It will be understood that, although the terms “first”, “second”, etc.may be used herein to describe various elements, components, regions,layers and/or sections, these elements, components, regions, layersand/or sections should not be limited by these terms. These terms areonly used to distinguish one element, component, region, layer orsection from another element, component, region, layer or section. Thus,a first element, component, region, layer or section discussed belowcould be termed a second element, component, region, layer or sectionwithout departing from the teachings of example embodiments.

Spatially relative terms, such as “beneath,” “below,” “lower,” “above,”“upper” and the like, may be used herein for ease of description todescribe one element or feature's relationship to another element(s) orfeature(s) as illustrated in the figures. It will be understood that thespatially relative terms are intended to encompass differentorientations of the device in use or operation in addition to theorientation depicted in the figures. For example, if the device in thefigures is turned over, elements described as “below” or “beneath” otherelements or features would then be oriented “above” the other elementsor features. Thus, the exemplary term “below” can encompass both anorientation of above and below. The device may be otherwise oriented(rotated 90 degrees or at other orientations) and the spatially relativedescriptors used herein interpreted accordingly.

The terminology used herein is for the purpose of describing exemplaryembodiments only and is not intended to be limiting of exampleembodiments. As used herein, the singular forms “a,” an and the areintended to include the plural forms as well, unless the context clearlyindicates otherwise. It will be further understood that the terms“comprises” and/or “comprising,” when used in this specification,specify the presence of stated features, integers, steps, operations,elements, and/or components, but do not preclude the presence oraddition of one or more other features, integers, steps, operations,elements, components, and/or groups thereof.

Example embodiments are described herein with reference tocross-sectional illustrations that are schematic illustrations ofidealized embodiments (and intermediate structures) of exampleembodiments. As such, variations from the shapes of the illustrations asa result, for example, of manufacturing techniques and/or tolerances,are to be expected. Thus, example embodiments should not be construed aslimited to the particular shapes of regions illustrated herein but areto include deviations in shapes that result, for example, frommanufacturing. For example, an implanted region illustrated as arectangle will, typically, have rounded or curved features and/or agradient of implant concentration at its edges rather than a binarychange from implanted to non-implanted region. Likewise, a buried regionformed by implantation may result in some implantation in the regionbetween the buried region and the surface through which the implantationtakes place. Thus, the regions illustrated in the figures are schematicin nature and their shapes are not intended to illustrate the actualshape of a region of a device and are not intended to limit the scope ofexample embodiments.

Unless otherwise defined, all terms (including technical and scientificterms) used herein have the same meaning as commonly understood by oneof ordinary skill in the art to which example embodiments belong. Itwill be further understood that terms, such as those defined incommonly-used dictionaries, should be interpreted as having a meaningthat is consistent with their meaning in the context of the relevant artand will not be interpreted in an idealized or overly formal senseunless expressly so defined herein.

Example embodiments provide a method of preparing graphene that includessupplying a gas including CO₂, CH₄, and H₂O to a metal catalyst forgraphene growth and reacting them by heating, and cooling the resultant.

The metal catalyst may be a transition metal catalyst having relativelyhigh adsorbability for carbon, specifically, at least one metal selectedfrom Ni, Co, Fe, Pt, Au, Al, Cr, Cu, Mg, Mn, Mo, Rh, Si, Sn, Ta, Ti, W,U, V, Zr, brass, bronze, stainless steel, and Ge, or an alloy catalyst,more specifically an alloy catalyst including Ni, Co, Cu, Fe, or two ormore of the aforementioned metals, and still more specifically, themetal catalyst may be a Ni catalyst.

The CH₄:CO₂:H₂O gases may be used in a mole ratio of about1:0.20-0.50:0.01-1.45, specifically, about 1:0.25-0.45:0.10-1.35, andmore specifically, about 1:0.30-0.40:0.50-1.0.

As shown in the reaction ratio, water is required to be included in anamount of at least greater than or equal to about 0.01, but when thewater is included in an amount of greater than or equal to about 1.45,carbon is not accumulated on the catalyst but is all converted into CO₂,and in addition, the Ni catalyst is completely oxidized, loweringreactivity and thus making it difficult to form graphene.

The heating may be performed at about 400 to about 900° C.,specifically, about 500 to about 850° C., and more specifically, about600 to about 800° C.

The cooling may be performed at a given rate in the presence of an inertgas, for example, nitrogen (N₂), argon (Ar), or helium (He) gas.

In example embodiments, the metal catalyst may be supported on acarrier, for example, a porous carrier or silicon.

The porous carrier may be an oxide carrier, e.g., Al₂O₃, SiO₂, zeolite,or TiO₂, for example, Al₂O₃.

The silicon may be amorphous silicon, and specifically, a semiconductorwafer.

The metal catalyst may be supported on the carrier in a form that themetal catalyst is adsorbed as spherical nanoparticles on the porouscarrier or bonded as ovals, or as asymmetric hexagonal prismaticnanoparticles on the porous carrier in a form of an alloy.

Otherwise, the metal catalyst may be supported on a semiconductor waferby depositing a metal using a CVD (chemical vapor deposition) method.

As described below in detail, the “composite” of the catalyst metalparticles with the porous carrier indicates that each catalyst particleis adhered to an carrier and forms a strong bond therewith throughstrong interaction between catalyst particles and the carrier and has acircular or oval cross-section when the alloy is vertically cut, asshown in the exaggerated view of FIG. 2(b).

On the other hand, a method of supporting a metal catalyst on a porouscarrier is well-known in a related art.

For example, the method of supporting a metal catalyst on a porouscarrier may include depositing at least one metal or an alloy selectedfrom Ni, Co, Fe, Pt, Au, Al, Cr, Cu, Mg, Mn, Mo, Rh, Si, Sn, Ta, Ti, W,U, V, Zr, brass, bronze, stainless steel, and Ge as a catalyst forgraphene growth on a carrier, specifically, a porous carrier by using athermal evaporator, an e-beam evaporator, a sputterer, or throughelectro-plating, or physically adsorbing the metal catalyst particlesfor graphene growth on the carrier in a wet method.

For example, the deposition of the metal catalyst particles on a porouscarrier using a wet method includes impregnating a porous carrier in anaqueous solution in which a metal catalyst is dissolved, heating thecarrier-coated catalyst in an oven, and drying it, and then firing theresultant at a relatively high temperature, reducing the fired catalystunder an inert gas atmosphere while heating at a predetermined or givenrate, and then maintaining the reduced catalyst at a relatively hightemperature under a hydrogen atmosphere to prepare a catalyst.

FIG. 1 (left) shows that the spherical metal catalyst particles arephysically adsorbed on the porous carrier in the prepared catalyst.

On the other hand, the metal catalyst particles may be strongly bondedwith the carrier in a form of an alloy as shown in FIG. 1 (right),rather than physically adsorbed on the porous carrier, while stillmaintaining a spherical shape.

In other words, as shown in FIG. 1 (right), when the metal catalystparticles are more strongly bonded with the porous carrier in a form ofan alloy than physically and chemically bonded therewith, the metalcatalyst particles have a hemispherical, oval, or upside down boat shaperather than the spherical shape, and thus more widely contact thesurface of the porous carrier and have a stronger bond.

FIGS. 2(a)-2(b) are exaggerated enlarged views of each catalyst particleto show a bonding form of the metal catalyst with the porous carrier.

As shown in FIG. 2(a), when the catalyst metal particles are physicallyadsorbed on the porous carrier, the catalyst metal particles have aspherical shape and a relatively smaller contact area with the porouscarrier.

On the other hand, as shown in FIG. 2(b), when the catalyst metalparticles are bonded with the porous carrier in a form of an composite,each catalyst metal particle has a semi-oval or upside down boat shapeand a relatively much larger contact area with the porous carriercompared with the contact area shown in FIG. 2(a).

As shown in the FIG. 2(b), the method of fusing the catalyst metalparticles with the porous carrier in a form of an metal particle-carriercomposite may include a process of cooling down a reactor having thecatalyst to room temperature and adding a small amount of water theretobefore heating under a hydrogen atmosphere as the last step forpreparing the catalyst.

In other words, when the catalyst is adsorbed on the porous carrieraccording to the aforementioned wet method, and water in a small amountis added to the catalyst metal particles, the catalyst metal particlesare pushed and crushed down by the water and thus have an oval shape andare more strongly bonded on the surface of the porous carrier.

In this way, when the catalyst metal particles are bonded with theporous carrier in a form of a composite, the catalyst particles have alarger contact area with the carrier and become more stable at arelatively high temperature. In addition, as described below in detail,carbon atoms are more easily adsorbed into a larger contact interfacebetween the catalyst and carrier, and accordingly, extra carbon atomsare not be accumulated on the surface of the catalyst but react withwater and produce CO and H₂ gas and thus prevent or reduce deteriorationof the catalyst by coking of the catalyst.

Furthermore, as the carrier/catalyst has a larger interface area, a CO₂modifying reaction has higher efficiency on the interface.

FIG. 5 schematically shows this mechanism.

As shown in FIG. 5, when the catalyst metal particles are bonded withthe porous carrier in a form of an composite according to exampleembodiments, this catalyst more effectively has a CO₂ modify reactionthrough the larger interface between the carrier/catalyst, but furtherdecreases coking and deterioration of the catalyst as a side reactiondue to accumulation of carbon on the surface of the catalyst particles.

Accordingly, a composite catalyst of a catalyst/a carrier forms grapheneat a higher rate than a non-composite catalyst of a catalyst/a carrier.

Specifically, the non-composite catalyst has several-layered graphene onthe surface of catalyst particles, while the composite catalyst hassingle layered or 2- or 3-layered graphene on the surface of thecatalyst particles.

As aforementioned, the catalyst particles may be bonded with the porouscarrier to form a composite according to example embodiments, but arenot limited thereto, and may be variously supported on the carrier toform graphene.

The metal catalyst may be supported in an amount of about 1 to about 50wt %, specifically, about 3 to about 20 wt %, and more specifically,about 5 to about 12 wt % on the oxide carrier.

As aforementioned, the conventional chemical vapor deposition formsgraphene on the surface of a catalyst layer due to a melting temperaturedifference between the catalyst and carbon by reacting a mixed gas ofCH₄ and hydrogen at a relatively high temperature (about 1000° C.) sothat carbon may be adsorbed in a transition metal (Ni or Cu) catalystlayer deposited on a substrate and then cooling down the resultant, butthis requires a relatively difficult process of adjusting theconcentration of the mixed gas so that an appropriate amount of carbonflows in the catalyst layer, a cooling rate for taking out the carbonfrom the surface of the catalyst layer and forming graphene thereon, anda thickness of the catalyst layer.

For example, as shown in FIG. 3, the cooling rate may bring about asubstantial yield difference in that carbon comes out of the catalystlayer and forms graphene.

Specifically, when the cooling rate is too fast, the cooling may becomplete before carbon atoms come out of the surface of the catalystlayer, while when the cooling is too slow, carbon atoms may not formgraphene but fly away.

Accordingly, a medium cooling rate is appropriate for forming graphene,but is hard to control.

According to example embodiments, carbon dioxide (CO₂) and methane (CH₄)gases are used as a carbon source and water (H₂O) is used as a necessaryreactant to prevent or reduce a coking phenomenon, as extra carbon atomsforming no graphene out of the molten carbon or escaping the catalystlayer react with oxygen (O) atoms in the water and produce CO and H₂gases, otherwise the extra carbon atoms will be accumulated on thesurface of the catalyst layer with a whisker shape.

Accordingly, the catalyst is used for a continuous process for forminggraphene.

FIG. 4 schematically shows interaction of the carbon atom source (CO₂and CH₄) with the water on the surface of the catalyst, and thenconversion of extra carbon atoms therefrom and the water into CO and H₂gases and evaporation thereof from the catalyst.

On the other hand, the extra carbon atoms are melted into the catalystlayer rather than coking on the surface of the catalyst layer and thusform a catalyst interstitial layer in the catalyst layer, and thecatalyst interstitial layer comes out of the surface of the catalystlayer by cooling after the reaction and forms graphene.

The graphene formation is schematically shown in FIG. 5.

The reaction between the water and the carbon atom source may beappropriately performed in the above mole ratio of the CH₄:CO₂:H₂Ogases, but is not limited thereto, and the CH₄, CO₂, and H₂O gases maybe appropriately provided within the ratio range to prevent or reducethe extra carbon atoms from coking on the catalyst layer.

On the other hand, the coking prevention or reduction effect may beaccomplished by directly injecting water (H₂O) along with CH₄ and CO₂gases according to example embodiments, or by adding a materialproducing water during the reaction without directly injecting the water(H₂O).

In other words, when alcohol in an appropriate amount is added with theCH₄ and CO₂ gases, these additives may be heated to decompose thealcohol and produce water, bringing about the same effect.

Accordingly, the reaction may be performed by using a compoundrepresented by C_(x)H_(y)O_(z) capable of being converted into waterduring the heating in the same ratio as water in the reactant, insteadof water.

As described above, the metal catalyst may be supported in a form ofmetal nanoparticles, specifically with a spherical, hemispherical, oval,or asymmetric hexagonal prismatic shape, on the carrier.

As described above, when the metal catalyst particles are bonded on thecarrier to form a composite, the metal catalyst particles have a largerbonding area with the porous carrier and higher efficiency of producinggraphene on the surface of the metal catalyst particles having thelarger bonding area with the carrier.

Without being bound to a specific theory, graphene is formed by carbonmelted into a catalyst layer through an interface between the catalystand carrier.

Accordingly, as shown in FIG. 2(a), since the metal catalyst particlesare not just adsorbed on the carrier while maintaining a spherical shapethemselves but are strongly bonded with the carrier in a form of acomposite, the composite catalyst having a larger interface area betweenthe catalyst and carrier may more efficiently form graphene on thesurface of the catalyst.

In addition, since CO and H₂ gases are produced and evaporated by areaction of extra carbon with water on the interface, a cokingphenomenon in which carbon atoms are accumulated on the surface of thecatalyst and coke the catalyst may be more effectively prevented orreduced in the catalyst as shown in FIG. 2(b).

In example embodiments, the catalyst may be provided in a form of a filmor substrate, and a carrier supporting the catalyst may be provided onat least one part of the catalyst in the form of the film or substrate.

The carrier provided on the catalyst may be provided in a form of Al,Si, or Ti ions, and graphene may be produced where the carrier isprovided on the catalyst substrate or film by providing CO₂, CH₄, andH₂O gases.

The carrier ions may be provided on the catalyst substrate or film in amethod of sputtering a gas including Al, Si, or Ti ions on the catalystsubstrate or film or coating an aqueous solution including the carrierions on the catalyst substrate or film.

Specifically, a compound including the carrier ions is dissolved inwater to prepare an aqueous solution, and then the aqueous solution isspin-coated on a substrate. As described above, graphene is formed fromcarbon that is melted down into a catalyst layer through the interfacebetween the catalyst and carrier and thus the graphene is formed onlywhere the carrier, e.g., Al, Si, or Ti ions, is present on the catalystsubstrate or film.

According to example embodiments, when the carrier ions are provided ona part of the catalyst substrate or film, graphene is produced only onthe part of the substrate or film provided with the carrier ions.

If the carrier is provided with a pattern on the catalyst substrate orfilm, graphene is produced with the pattern on the substrate or film.

According to example embodiments, when the carrier is provided over theentire surface of the catalyst substrate or film, graphene is producedas a sheet on the entire surface of the substrate or film.

Accordingly, nanoparticles including the graphene, and a patternedgraphene or a graphene sheet on a metal catalyst substrate or filmprepared according to the method of preparing graphene, are provided.

Specifically, the nanoparticles including graphene may be metalnanoparticles encapsulated by graphene. For example, the metalnanoparticles encapsulated by graphene may be partially or entirelyencapsulated by graphene.

The metal nanoparticles partially or entirely encapsulated by graphenemay be prepared by preparing graphene on a surface of a metalnanoparticle supported on a porous carrier by using the method accordingto an embodiment. The obtained metal nanoparticle partially or entirelyencapsulated by graphene on the porous carrier may be released from theporous carrier by removal of the porous carrier with a well-known methodin the art, for instance, etching.

The metal nanoparticles may include at least one metal selected from Ni,Co, Cu, Fe, Rh, Ru, Pt, Au, Al, Cr, Mg, Mn, Mo, Si, Sn, Ta, Ti, W, U, V,Zr, brass, bronze, stainless steel, and Ge, or alloy nanoparticlesincluding two or more of the foregoing metals, specifically Ni, Co, Cu,Fe, or two or more of the foregoing metals.

The metal nanoparticles may have a spherical shape, hemispherical shape,oval shape, or asymmetric hexagonal prism shape, and specifically, themetal nanoparticles may have an asymmetric hexagonal prismatic shape.

In addition, the metal nanoparticles may have a diameter ranging fromabout 10 to about 50 nm, and specifically, from about 20 to about 40 nm,and when the metal nanoparticles have an oval or asymmetric hexagonalprismatic shape, the diameter is measured with reference to the longestdiameter in the cross-section of the nanoparticles.

The metal nanoparticles partially or entirely encapsulated by graphenemay be used as various electronic materials, e.g., a light emittingmaterial for a display, an electrode material of a battery or a solarcell, or a bio medicine material, e.g., drug delivery material in vivo.

Herein, the metal nanoparticles may particularly include magnetic metalnanoparticles, e.g., Fe, Co, Ni, or an alloy thereof.

On the other hand, when the metal nanoparticles encapsulated by grapheneare heated to melt out the metal nanoparticles, a hollow graphenenanoparticle is obtained.

Only the metal nanoparticles may be etched by using an oxidationetchant, for example, an iron (III) chloride (FeCl₃) aqueous solution (1M) in order to remove the metal nanoparticles and provide a hollowgraphene nanoparticle.

However, the etchant solution is not limited thereto.

The graphene or graphene sheet is patterned on the metal catalystsubstrate or film by providing at least a part of the substrate or filmwith Al, Si, or Ti ions and with CO₂, CH₄, and H₂O gases, heating andreacting them, and cooling the resultant to form graphene only where thepart of the substrate or film is provided with the Al, Si, or Ti ions.

Specifically, when the metal catalyst substrate or film is provided withthe carrier ions, graphene is produced only on a part of the catalystsubstrate or film where the carrier ions are provided.

Accordingly, when a carrier is provided with a pattern on a part of themetal catalyst substrate or film, graphene is formed with the patternwhere the carrier is provided.

FIG. 6 shows the graphene pattern formation.

Referring to FIG. 6, when Al ions are coated along letters of “SAIT” ona Ni film as a metal catalyst, provided with CO₂, CH₄, and H₂O gases,and then heated for a reaction and cooled down, a graphene film isformed in the letters “SAIT” provided with the Al ions.

Herein, the Ni film is etched using an etchant solution, leaving theletters “SAIT” formed of graphene.

The patterned graphene according to example embodiments may be used as acircuit or a semiconductor material.

In addition, a Ni film or substrate as a metal catalyst is providedoverall with a carrier, e.g., Al ions, and with CO₂, CH₄, and H₂O gasesand heated for a reaction and cooled down to form a graphene film allover the Ni film or substrate, and the Ni film or substrate is removedto obtain the graphene sheet.

The method may more easily provide a graphene sheet having a largetwo-dimensional area.

The patterned graphene or graphene sheet may be easily regulatedregarding thickness and shape by adjusting concentration of the carrierprovided on the metal catalyst substrate or film.

Hereinafter, the present disclosure is illustrated in more detail withreference to examples and comparative examples.

However, these examples and comparative examples are examples, and thepresent disclosure is not limited thereto.

EXAMPLE Preparation Example 1 Preparation of Catalyst for GrapheneGrowth (7 wt % Ni/γ-Al₂O₃)

A catalyst for graphene growth is prepared by supporting 7 wt % of a Nimetal catalyst on γ-Al₂O₃.

Specifically, alumina (150 m²/g, the diameter of an alumina granule:about 3 mm φ, Alfa) is impregnated in a Ni(NO₃)₂.H₂O (Samchun Chemical)aqueous solution, dried in a 120° C. oven for 24 hours, and fired at500° C. under an air atmosphere for 5 hours.

The fired catalyst is heated at a speed of 10° C./min and reduced undera nitrogen atmosphere, and then maintained at 850° C. under a hydrogenatmosphere, preparing a 7 wt % Ni/γ-Al₂O₃ catalyst.

The catalyst is cooled down to 30° C., and 5 ml of distilled water isadded thereto.

Then, the mixture is heated (at 10° C./min) to evaporate the watertherein under a hydrogen atmosphere and maintained at 850° C. for 1hour.

A 3D TEM image of the catalyst is taken to examine the shape of thesupported catalyst metal, and the cross-section of the supportedcatalyst metal is analyzed to evaluate the catalyst metal supported onthe carrier.

FIG. 7 shows the cross-section of the 3D TEM image.

The catalyst metal has a bonding cross-section of a spherical or ovalshape, which shows that catalyst particles have an interaction with thecarrier and thus form a composite bonding therewith.

Preparation Example 2 Preparation of Catalyst for Graphene Growth (7 wt% Ni/γ-Al₂O₃)

A 7 wt % Ni/γ-Al₂O₃ catalyst is prepared in an initial wet method.

Alumina (150 m²/g, the diameter of an alumina granule: about 3 mm φ,Alfa) is impregnated in a Ni(NO₃)₂.H₂O (Samchun Chemical) aqueoussolution, dried in an oven at 120° C. for 24 hours, and fired at 500° C.under an air atmosphere for 5 hours.

The fired catalyst is heated (at 10° C./min) and reduced under anitrogen atmosphere and then maintained at 850° C. under a hydrogenatmosphere for one hour, preparing a 7 wt % Ni/γ-Al₂O₃ catalyst.

A 3D TEM image photograph of the catalyst is taken to examine the shapeof the supported catalyst metal, and the cross-section of the supportedcatalyst metal is analyzed to evaluate the metal catalyst supported onthe carrier.

FIG. 8 shows the cross-section of the 3D TEM image.

The 3D TEM image shows that the catalyst metal has a spherical shape.

Preparation Example 3 Preparation of Catalyst for Graphene Growth (AlIon-Coated Catalyst on Ni Film)

0.1 g of an Al(NO₃)₃.9H₂O compound is dissolved in 3 ml of water, andthe aqueous solution is spin-coated on a Ni film at a speed of 300 rpmand fired in an 80° C. oven for 600 minutes, preparing a catalyst coatedwith Al ions on the Ni film.

Preparation Example 4 Preparation of Catalyst for Graphene Growth(Ni-Deposited Catalyst on Silicon Wafer)

A catalyst for graphene growth is prepared by depositing Ni to be 300 nmthick on a semiconductor silicon wafer in a CVD method.

Example 1 Preparation of Graphene-Encapsulated Ni Nanoparticles

While CH₄, CO₂, and water (H₂O) in a ratio of about 1:0.38:0.81 are putin 0.45 g of the 7 wt % Ni metal catalysts supported on γ-Al₂O₃according to Preparation Examples 1 and 2 at 700° C. at 1 atm under anitrogen (N₂) condition at 200 sccm (standard cubic centimeters perminute), a reaction is performed for about 10 hours (gas hourly spacevelocity (GHSV)=50,666 k cc/g·hr).

FIG. 9 is a TEM photograph showing the catalyst according to PreparationExample 1 after the reaction, and FIG. 10 is a TEM photograph showingthe catalyst according to Preparation Example 2 after the reaction.

As shown in the photograph of FIG. 9, the Ni metal catalyst has ahexagonal cross-section, and graphene is formed as a white monolayer ordouble layer along the external circumferential edge of the hexagonalcross-section.

The Ni particles have a diameter of about 35 to 40 nm.

FIG. 10 shows that a multiple layer graphene layer is formed on the Ninanoparticles.

In addition, a Raman peak in FIG. 11 and an XPS peak in FIG. 12 showthat graphene was formed on the catalysts.

Referring to FIG. 11, the catalyst according to Preparation Example 1has a smaller D/G peak surface area and a higher crystalline graphenelayer than the catalyst according to Preparation Example 2.

Referring to FIG. 12, the catalyst according to Preparation Example 1has a clearer C—C or C═C peak showing the graphene characteristic thanthe catalyst according to Preparation Example 2, and the catalystaccording to Preparation Example 2 has a metal carbide peak due to thewhisker-shaped carbon.

Example 2 Preparation of Patterned Graphene

While CH₄, CO₂, and water (H₂O) in a ratio of about 1:0.38:0.81 are putin the Ni film coated with Al ions according to Preparation Example 3 at700° C. at 1 atm under a nitrogen (N₂) condition for 2 hours at a speedof 200 sccm (standard cubic centimeters per minute), a reaction isperformed for about 2 hours (gas hourly space velocity (GHSV)=50,666 kcc/g·hr).

FIG. 13 is a SEM (scanning electron microscope) photograph showing agraphene layer on the Ni film after the reaction.

Based on the SEM photograph, graphene is found to be formed on an Alion-coated part of the Ni film.

FIG. 14 shows a Raman peak exhibiting that graphene is formed on an Alion-coated part of the Ni film.

Referring to FIG. 14, graphene has higher crystalline on the Alion-coated part of the Ni film than the non-coated part of the Ni film.

FIG. 15 is an XPS graph showing that graphene is formed on the Alion-coated part of the Ni film.

The XPS graph shows that graphene is formed as one layer, 2-3 layers, ora several layers depending on the concentration of Al.

Example 3 Preparation of Patterned Graphene

The specimen deposited to be 300 nm thick on a semiconductor wafer in aCVD method according to Preparation Example 4 is used as a catalyst forgraphene growth to form graphene by injecting CH₄ and H₂ therein atrespective speeds of 100 sccm and 200 sccm (standard cubic centimetersper minute), which is a conventional condition for producing graphene,and performing a reaction at 700° C. at 1 atm under a nitrogen (N₂)condition for 30 minutes, cooling down the graphene under an N₂atmosphere, and after the graphene layer is reacted with the gases ofCH₄:CO₂:H₂O in a ratio of 100 sccm:100 sccm:10 sccm, the surface of thegraphene layer is Raman-analyzed.

As a result of the analysis, as shown in FIG. 16, highly crystalline butless defective graphene is formed by adding CO₂ and H₂O.

In addition, FIG. 17 is a SEM (scanning electron microscope) photographshowing graphene produced on the Ni catalyst deposited on thesemiconductor wafer, and FIG. 17(b) is an enlargement of FIG. 17(a).

While this disclosure has been described in connection with what ispresently considered to be practical example embodiments, it is to beunderstood that the inventive concepts are not limited to the disclosedembodiments, but, on the contrary, is intended to cover variousmodifications and equivalent arrangements included within the spirit andscope of the appended claims.

What is claimed is:
 1. A graphene-encapsulated metal nanoparticle prepared by a method including supplying a gas on a metal catalyst, the gas including CO₂, CH₄, and H₂O; and reacting and cooling the resultant, wherein the supplying supplies the gas in a mole ratio of the CH₄, CO₂, and H₂O gases at about 1:0.20-0.50:0.01-1.45.
 2. The graphene-encapsulated metal nanoparticle of claim 1, wherein the metal nanoparticle includes at least one metal selected from Ni, Co, Cu, Fe, Rh, Ru, Pt, Au, Al, Cr, Mg, Mn, Mo, Si, Sn, Ta, Ti, W, U, V, Zr, brass, bronze, stainless steel, and Ge, or an alloy including two or more of the aforementioned metals.
 3. The graphene-encapsulated metal nanoparticle of claim 1, wherein the metal nanoparticle has a diameter of about 1 to about 50 nm.
 4. The graphene-encapsulated metal nanoparticle of claim 1, wherein the graphene-encapsulated metal nanoparticle is used in one of a light emitting material for a display, an electrode material of a battery or a solar cell, and an in vivo drug delivery material.
 5. A hollow graphene nanoparticle prepared by removing the metal nanoparticle from the graphene-encapsulated metal nanoparticle according to claim
 1. 